I've been fortunate in that, except with the first crash that brought on the diagnosis, I am able to work full-time. I work for DHS doing Food Assistance and Medicaid. At my last visit, my electrophysiologist prescribed a mobility scooter for when I want to go out - but not a work yet, changed my meds, and suggested that I no longer use a desk chair. I also have a wheelchair for those times my husband and I don't want to mess with the scooter. Instead of a desk chair, I use a large exercise ball as my chair. This way I have more movement and not as much blood pooling. Fortunately, I don't have to walk much for work. And I've told my teammates about my POTS. They wanted to know if they would need to call 9-1-1, so I told them "If I'm face down, call 9-1-1-. If I'm on my back, don't worry about it -- I put myself there." My teammates are good at noticing when I am in brain fog, lightheaded, etc., and taking care of me when I try to do too much. I miss work occasionly, or have to go home early, because of a POTS episode, but I miss less work than most of my co-workers who are "normal." Of course, the weekend is "crash" time. I rarely do any of the work around the house, because I conserve my strength so I can continue to work.